Efficacy and Safety of Gadopiclenol for Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

Status: complete

This trial aimed to evaluate the Efficacy and Safety of gadopiclenol for Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

Patient presenting with known or highly suspected CNS lesion(s) with focal areas of disrupted Blood Brain Barrier (BBB) (e.g., primary and secondary tumors) based on results of a previous imaging procedure such as Computed Tomography (CT) or MRI, which should have been performed within 12 months prior to ICF signature.

Patient presenting with acute or chronic renal insufficiency, defined as an estimated Glomerular Filtration Rate (eGFR) < 30 mL/min/1.73 m² assessed within 1 day prior to each contrast agent injection
Patient presenting extra cranial lesions and/or extra-dural lesions.

The purpose of this trial was to evaluate a new gadolinium-based contrast agent (GBCA)

gadopiclenol injection for Central Nervous System (CNS) lesion detection and

visualization by conventional steady-state CNS imaging.

This is a multi-center, international, prospective, double-blind, randomized, controlled,

cross-over with comparator trial in male and female patients presenting with known or

highly suspected CNS lesion(s) with focal areas of disrupted Blood Brain Barrier (BBB)

(e.g., primary and secondary tumors) who are scheduled to undergo a routine

contrast-enhanced Magnetic Resonance Imaging (MRI) of the CNS.

This trial was conducted in 33 centers worldwide.

During the course of the trial, two MRIs were obtained from each patient: one unenhanced

and gadopiclenol-enhanced MRI; and one unenhanced and gadobutrol-enhanced MRI. MRI

evaluations were performed by on-site investigators and three independent off-site

blinded readers.

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